The 11-year long-term follow-up study from the randomized BENEFIT CIS trial

Ludwig Kappos(Düsseldorf University Hospital), Gilles Edan(Düsseldorf University Hospital), Mark S. Freedman(Düsseldorf University Hospital), Xavier Montalbán(Düsseldorf University Hospital), Hans‐Peter Hartung(Düsseldorf University Hospital), Bernhard Hemmer(Düsseldorf University Hospital), Edward Fox(Düsseldorf University Hospital), Frederik Barkhof(Düsseldorf University Hospital), Sven Schippling(Düsseldorf University Hospital), Andrea Schulze(Düsseldorf University Hospital), Dirk Pleimes(Düsseldorf University Hospital), Christoph Pohl(Düsseldorf University Hospital), Rupert Sandbrink(Düsseldorf University Hospital), Gustavo Cruz(Düsseldorf University Hospital), Eva‐Maria Wicklein(Düsseldorf University Hospital), For the BENEFIT Study Group(Düsseldorf University Hospital), BENEFIT Study Group, Siegrid Strasser‐Fuchs, Thomas Berger, K. Vass, Christian Sindic, Bénédicte Dubois, Dominique Dive, Valérie Delvaux, Jason P. DeBruyne, Luanne M. Metz, G Rice, Marcelo Kremenchutzky, Pierre Duquette, Yves Lapierre, Mark Freedman(Düsseldorf University Hospital), Anthony Traboulsee, Paul O’Connor, Pavel Štourač, Radomír Taláb, Martin Vališ, Olga Zapletalová, I Kovarova, Eva Medová, Jiří Fiedler, Jette Lautrup Frederiksen, Bruno Brochet, T. Moreau, Patrick Vermersch, Jean Pelletier, G Edan(Düsseldorf University Hospital), Michel Clanet, B David, Pierre Clavelou, Christine Lebrun‐Frénay, Olivier Gout, Mikko Kallela, Tuula Pirttilä, Juhani Ruutiainen, J-P Erälinna, Keijo Koivisto, Mauri Reunanen, I Keskinarkus, Irina Elovaara, Arno Villringer, H. Altenkirch, Lars Bauer, M Ghazi, C Pohl(Düsseldorf University Hospital), K. Wessel, HP Hartung(Düsseldorf University Hospital), Wolfgang Steinke, B. C. Kieseier, Hans Wolfgang Kölmel, Patrick Oschmann, Martin Berghoff, Ricarda Diem, B. Kitze, Alexander Dressel, Francine Hoffmann, K. Baum, Simon Jung, H.-F. Petereit, D. Reske, Michael Sailer, Jürgen Köhler, Björn Tackenberg, Luisa Klotz, Reinhard Hohlfeld, Tania Kuempfel, K.T. Henn, Andreas Steinbrecher, Klemens Angstwurm, Hayrettin Tumani, Ralf Gold, P Rieckmann, Christoph Kleinschnitz, R Komoly, G Gács, Gábor Jakab, Gyula Pánczél, Tünde Csépány, László Csiba, László Vécsei, Ariel Miller, Dimitrios Karussis, Joab Chapman, Angelo Ghezzi, Gıancarlo Comı, V. Martinelli, Paolo Gallo, V. Cosi, Roberto Bergamaschi, Luca Durelli, Paola Cavalla, CH Polman, Frederik Barkhof(Düsseldorf University Hospital), Bernard M.J. Uitdehaag, Bert Anten, Raymond Hupperts, Leo H. Visser, K-M Myhr, Andrzej Szczudlik, Krzysztof Selmaj, Zbigniew Stelmasiak, Halina BarosikPsujek, Ryszard Podemski, Zdzisław Maciejek, Sławomir Wawrzyniak, Luı́s Cunha, Saša Šega‐Jazbec, Xavier Montalbán(Düsseldorf University Hospital), T. Arbizu, Albert Saiz Hinarejos, José Antonio Bárcena, Sergio Martínez‐Yélamos, Roberto Alcázar Arroyo, Óscar Fernández, Guillermo Izquierdo Ayuso, Bonaventura Casanova Estruch, Jan Lycke, Ludwig Kappos(Düsseldorf University Hospital), A de Vera, S Wu, EW Radue, Jens Kühle, Heinrich P. Mattle, Karl T. Beer, Robert E. Coleman, D. H. Miller, Jeremy Chataway, J O’Riordan, Stephen Howell, G Edan(Düsseldorf University Hospital), Mark Freedman(Düsseldorf University Hospital), HP Hartung(Düsseldorf University Hospital), Ludwig Kappos(Düsseldorf University Hospital), D. H. Miller, Xavier Montalbán(Düsseldorf University Hospital), CH Polman, Lars Bauer, M Ghazi, C Pohl(Düsseldorf University Hospital), CH Polman, F Barkhof(Düsseldorf University Hospital), Bernard M.J. Uitdehaag, Ludwig Kappos(Düsseldorf University Hospital), A de Vera, S Wu, F Barkhof(Düsseldorf University Hospital), EW Radue, H. McFarland, Jürg Kesselring, A. John Petkau, Toyka Kv
Neurology
August 16, 2016
Cited by 130Open Access
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Abstract

OBJECTIVE: To assess outcomes for patients treated with interferon beta-1b immediately after clinically isolated syndrome (CIS) or after a short delay. METHODS: Participants in BENEFIT (Betaferon/Betaseron in Newly Emerging MS for Initial Treatment) were randomly assigned to receive interferon beta-1b (early treatment) or placebo (delayed treatment). After conversion to clinically definite multiple sclerosis (CDMS) or 2 years, patients on placebo could switch to interferon beta-1b or another treatment. Eleven years after randomization, patients were reassessed. RESULTS: Two hundred seventy-eight (59.4%) of the original 468 patients (71.3% of those eligible at participating sites) were enrolled (early: 167 [57.2%]; delayed: 111 [63.1%]). After 11 years, risk of CDMS remained lower in the early-treatment arm compared with the delayed-treatment arm (p = 0.0012), with longer time to first relapse (median [Q1, Q3] days: 1,888 [540, not reached] vs 931 [253, 3,296]; p = 0.0005) and lower overall annualized relapse rate (0.21 vs 0.26; p = 0.0018). Only 25 patients (5.9%, overall; early, 4.5%; delayed, 8.3%) converted to secondary progressive multiple sclerosis. Expanded Disability Status Scale scores remained low and stable, with no difference between treatment arms (median [Q1, Q3]: 2.0 [1.0, 3.0]). The early-treatment group had better Paced Auditory Serial Addition Task-3 total scores (p = 0.0070). Employment rates remained high, and health resource utilization tended to be low in both groups. MRI metrics did not differ between groups. CONCLUSIONS: Although the delay in treatment was relatively short, several clinical outcomes favored earlier treatment. Along with low rates of disability and disease progression in both groups, this supports the value of treatment at CIS. CLINICALTRIALSGOV IDENTIFIER: NCT01795872. CLASSIFICATION OF EVIDENCE: This study provides Class IV evidence that early compared to delayed treatment prolongs time to CDMS in CIS after 11 years.


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